Information for journalists

We welcome any interest in the condition from journalists. Feel free to use information on the site, all of which is backed by research (unless otherwise stated). Please cite us as your source if you do this and put details of our website address in the copy. We are also happy to check copy of any articles written to ensure that the information is accurate and up to date.


General enquiries

For general enquiries contact Jenny Chambers (07843 660349;, Founder. Jenny also works in research into the condition at Imperial College and King’s College London.

Case studies

We are able to provide case studies for articles on ICP. Please contact Jenny Chambers ( if you would like to be put in touch with someone who has been affected by the condition.

Key facts

Intrahepatic cholestasis of pregnancy (also known as obstetric cholestasis, or OC) affects 1 in 140 women (0.7%, or around 5,500 women) in the UK every year.

The cause of ICP is not fully understood but is likely to be multifactorial:

  • Hormones are implicated, as women expecting twins (or more, e.g. triplets) seem to be predisposed towards developing the condition, as are women who have had IVF.
  • The condition has a genetic component, as researchers know that mothers, daughters and sisters of affected women have a higher than average risk of being affected. Research has so far identified several gene mutations involved in ICP.
  • The condition appears to have a seasonal trend, with higher numbers in the winter months than in summer, suggesting that environmental factors such as sunlight or diet could be implicated.

Main symptoms include:

  • Itching – often on the hands and feet, but it can occur anywhere on the body and is typically worse at night. It can range in intensity from mild to so severe that the woman scratches herself until she breaks the skin and makes herself bleed.
  • Dark urine – women often report that their urine becomes darker.
  • Pale stools – a small number of women develop pale stools (also known as steatorrhea).


  • It usually presents in the third trimester of pregnancy, but can be earlier (as early as the first trimester).
  • It is possible to itch for some time before liver functions tests show any abnormalities or bile acid levels become elevated.

It should be diagnosed by:

  • Blood tests: liver function test and bile acids levels.
  • Excluding other possible causes such as autoimmune hepatitis, PBC (primary biliary cholangitis) and other liver disorders.

It is associated with:

  • Meconium staining of the amniotic fluid.
  • Spontaneous premature labour.
  • Fetal distress.
  • In severe cases, stillbirth (thought to be associated with high bile acid levels).

It is typically treated and managed by:

Note: This section will be updated in light of the research by Chappell et al 2019, which shows that UDCA is not an effective treatment for ICP.

  • Prescribing medication such as ursodeoxycholic acid and, in severe cases, rifampicin (although this drug should only be given in conjunction with specialist advice).
  • Delivering the baby at around 37–38 weeks.
  • Large trials are still required to validate these as best practice.


The information above is based on the following list of selected academic publications about ICP.

Abedin P, Weaver JB, Egginton E. Intrahepatic cholestasis of pregnancy: prevalence and ethnic distribution. Ethn Health 1999; 4: 35–37

Chappell LC, Gurung V, Seed PT, Chambers J, Williamson C, Thornton JG. Ursodeoxycholic acid versus placebo, and early term delivery versus expectant management, in women with intrahepatic cholestasis of pregnancy: semifactorial randomised clinical trial. BMJ 2012; 344 doi: 10.1136/bmj.e3799

Dixon PH, van Mil SW, Chambers J, Strautnieks S, Thompson RJ, Lammert F, Kubitz R, Keitel V, Glantz A, Mattsson LA, Marschall HU, Molokhia M, Moore GE, Linton KJ, Williamson C. Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy. Gut 2009; 58: 537–544

Dixon PH, Williamson C. The molecular genetics of intrahepatic cholestasis of pregnancy. Obstet Med 2008; 1: 65–71

Fisk NM, Story GM. Fetal outcome in obstetric cholestasis. Br J Obstet Gynaecol 1988; 95 1137–1143

Geenes V, Williamson C. Intrahepatic cholestasis of pregnancy. World J Gastroenterol 2009 May 7; 15(17): 2049–2066

Glantz A, Marschall HU, Mattsson LA. Intrahepatic cholestasis of pregnancy: relationships between bile acid levels and fetal complication rates. Hepatology 2004; 40: 467–474

Heikkinen J. Serum bile acids in the early diagnosis of intrahepatic cholestasis of pregnancy. Obstet Gynecol 1983.

Kenyon AP, Piercy CN, Girling J, Williamson C, Tribe RM, Shennan AH. Obstetric cholestasis, outcome with active management: a series of 70 cases. BJOG 2002; 109: 282–288

Laatikainen T, Ikonen E. Fetal prognosis in obstetric hepatosis. Ann Chir Gynaecol Fenn 1975; 64: 155–164 

Laatikainen T, Tulenheimo A. Maternal serum bile acid levels and fetal distress in cholestasis of pregnancy. Int J Gynaecol Obstet 1984; 22: 91–94

Lee RH, Kwok KM, Ingles S, Wilson ML, Mullin P, Incerpi M, Pathak B, Goodwin TM. Pregnancy outcomes during an era of aggressive management for intrahepatic cholestasis of pregnancy. Am J Perinatol 2008; 25: 341–345

Marschall HU, Wagner M, Zollner G, Fickert P, Diczfalusy U, Gumhold J, Silbert D, Fuchsbichler A, Benthin L, Grundström R, Gustafsson U, Sahlin S, Einarsson C, Trauner M. Complementary stimulation of hepatobiliary transport and detoxification systems by rifampicin and ursodeoxycholic acid in humans. Gastroenterology 2005; 129: 476–485

Palma J, Reyes H, Ribalta J, Iglesias J, Gonzalez MC, Hernandez I, Alvarez C, Molina C, Danitz AM. Effects of ursodeoxycholic acid in patients with intrahepatic cholestasis of pregnancy. Hepatology 1992; 15: 1043–1047 

Reid R, Ivey KJ, Rencoret RH, Storey B. Fetal complications of obstetric cholestasis. Br Med J 1976; 1: 870–872

Reyes, H. Sex hormones and bile acids in intrahepatic cholestasis of pregnancy. Hepatology 2008; 47: 376–379

Roncaglia N, Arreghini A, Locatelli A, Bellini P, Andreotti C, Ghidini A. Obstetric cholestasis: outcome with active management. Eur J Obstet Gynecol Reprod Biol 2002; 100: 167–170

Saleh M, Abdo K. Consensus on the management of obstetric cholestasis: National UK survey. BJOG 2007; 114: 99–103

Sjövall K, Sjövall J. Serum bile acid levels in pregnancy with pruritus (bile acids and steroids 158). Clin Chim Acta 1966; 13: 207–211

Walker IA, Nelson-Piercy C, Williamson C. Role of bile acid measurement in pregnancy. Ann Clin Biochem 2002; 39: 105–113

Williamson C, Geenes V Intrahepatic cholestasis of pregnancy. Obstet Gynecol 2014; 124:120–133. DOI: 10.1097/AOG.0000000000000346.

Williamson C, Hems LM, Goulis DG, Walker I, Chambers J, Donaldson O, Swiet M, Johnston DG. Clinical outcome in a series of cases of obstetric cholestasis identified via a patient support group. BJOG 2004; 111: 676–681